Related references
Note: Only part of the references are listed.BAX and BAK1 are dispensable for ABT-737-induced dissociation of the BCL2-BECN1 complex and autophagy
Jose Manuel Bravo-San Pedro et al.
AUTOPHAGY (2015)
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
Axel Freischmidt et al.
NATURE NEUROSCIENCE (2015)
The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis
Johnathan Cooper-Knock et al.
NEUROTHERAPEUTICS (2015)
Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
Johan Bergh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
SOD1 aggregation in ALS mice shows simplistic test tube behavior
Lisa Lang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli et al.
SCIENCE (2015)
Pathogenic role of BECN1/Beclin 1 in the development of amyotrophic lateral sclerosis
Melissa Nassif et al.
AUTOPHAGY (2014)
Motor neuron disease and frontotemporal dementia: sometimes related, sometimes not
John Hardy et al.
EXPERIMENTAL NEUROLOGY (2014)
Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanisms
Leslie I. Grad et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Targeting autophagy in neurodegenerative diseases
Rene L. Vidal et al.
TRENDS IN PHARMACOLOGICAL SCIENCES (2014)
Beclin 1 Is Required for Neuron Viability and Regulates Endosome Pathways via the UVRAG-VPS34 Complex
Nicole C. McKnight et al.
PLOS GENETICS (2014)
Ubiquitination and selective autophagy
S. Shaid et al.
CELL DEATH AND DIFFERENTIATION (2013)
Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis
Karin S. Graffmo et al.
HUMAN MOLECULAR GENETICS (2013)
Dysregulation of intracellular copper homeostasis is common to transgenic mice expressing human mutant superoxide dismutase-1s regardless of their copper-binding abilities
Eiichi Tokuda et al.
NEUROBIOLOGY OF DISEASE (2013)
Composition of Soluble Misfolded Superoxide Dismutase-1 in Murine Models of Amyotrophic Lateral Sclerosis
Per Zetterstrom et al.
NEUROMOLECULAR MEDICINE (2013)
Microglial Beclin 1 Regulates Retromer Trafficking and Phagocytosis and Is Impaired in Alzheimer's Disease
Kurt M. Lucin et al.
NEURON (2013)
Autophagy in Human Health and Disease REPLY
Augustine M. K. Choi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
MECHANISMS OF DISEASE Autophagy in Human Health and Disease
Augustine M. K. Choi et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Fibrillation precursor of superoxide dismutase 1 revealed by gradual tuning of the protein-folding equilibrium
Lisa Lang et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis
Karin Forsberg et al.
ACTA NEUROPATHOLOGICA (2011)
Rapamycin treatment augments motor neuron degeneration in SOD1G93A mouse model of amyotrophic lateral sclerosis
Xiaojie Zhang et al.
AUTOPHAGY (2011)
Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
Peter M. Andersen et al.
NATURE REVIEWS NEUROLOGY (2011)
Proteasomal activity in skeletal muscle: A matter of assay design, muscle type, and age
Karl-Heinz Strucksberg et al.
ANALYTICAL BIOCHEMISTRY (2010)
Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
Daryl A. Bosco et al.
NATURE NEUROSCIENCE (2010)
Novel Antibodies Reveal Inclusions Containing Non-Native SOD1 in Sporadic ALS Patients
Karin Forsberg et al.
PLOS ONE (2010)
Analysis of proteome dynamics in the mouse brain
John C. Price et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
XBP-1 deficiency in the nervous system protects against amyotrophic lateral sclerosis by increasing autophagy
Claudio Hetz et al.
GENES & DEVELOPMENT (2009)
Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
Hristelina Ilieva et al.
JOURNAL OF CELL BIOLOGY (2009)
Autophagy Inhibition Compromises Degradation of Ubiquitin-Proteasome Pathway Substrates
Viktor I. Korolchuk et al.
MOLECULAR CELL (2009)
Two Beclin 1-binding proteins, Atg14L and Rubicon, reciprocally regulate autophagy at different stages
Kohichi Matsunaga et al.
NATURE CELL BIOLOGY (2009)
Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation
P. Andreas Jonsson et al.
NEUROBIOLOGY OF DISEASE (2009)
ALS motor phenotype heterogeneity, focality, and spread Deconstructing motor neuron degeneration
John M. Ravits et al.
NEUROLOGY (2009)
Bcl-2 complexed with Beclin-1 maintains full anti-apoptotic function
I. A. Ciechomska et al.
ONCOGENE (2009)
Gamma and alpha motor neurons distinguished by expression of transcription factor Err3
Andreas Friese et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
ALSOD: The Amyotrophic Lateral Sclerosis Online Database
Richard Wroe et al.
AMYOTROPHIC LATERAL SCLEROSIS (2008)
Inclusions of amyotrophic lateral sclerosis-linked superoxide dismutase in ventral horns, liver, and kidney
P. Andreas Jonsson et al.
ANNALS OF NEUROLOGY (2008)
Autophagy induction and autophagosome clearance in neurons: Relationship to autophagic pathology in Alzheimer's disease
Barry Boland et al.
JOURNAL OF NEUROSCIENCE (2008)
Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis
Julie D. Atkin et al.
NEUROBIOLOGY OF DISEASE (2008)
The autophagy effector Beclin 1: a novel BH3-only protein
S. Sinha et al.
ONCOGENE (2008)
Lysosomal membrane permeabilization in cell death
P. Boya et al.
ONCOGENE (2008)
Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases
Jeanne M. M. Tan et al.
HUMAN MOLECULAR GENETICS (2008)
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice
Masaaki Komatsu et al.
CELL (2007)
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models
Per Zetterstrom et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Complete dissociation of motor neuron death from motor dysfunction by Bax deletion in a mouse model of ALS
Thomas W. Gould et al.
JOURNAL OF NEUROSCIENCE (2006)
Onset and progression in inherited ALS determined by motor neurons and microglia
Severine Boillee et al.
SCIENCE (2006)
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy
HG Stewart et al.
MUSCLE & NERVE (2006)
Overloading of stable and exclusion of unstable human superoxide dismutase-1 variants in mitochondria of murine amyotrophic lateral sclerosis models
D Bergemalm et al.
JOURNAL OF NEUROSCIENCE (2006)
Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models
PA Jonsson et al.
BRAIN (2006)
Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosis
PA Jonsson et al.
BRAIN (2004)
Mutant dynactin in motor neuron disease
I Puls et al.
NATURE GENETICS (2003)
El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
BR Brooks et al.
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2000)
New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes
S Kato et al.
AMYOTROPHIC LATERAL SCLEROSIS (2000)